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KCNJ10
| Symbol: | KCNJ10 | | Name(s): | potassium inwardly-rectifying channel, subfamily J, member 10 | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1 | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 12401729 |
Observational study of gene-disease association. (HuGE Navigator) |
| 15120748 |
Observational study of gene-disease association. (HuGE Navigator) |
| 15725393 |
Observational study of gene-disease association. (HuGE Navigator) |
| 15911117 |
Observational study of gene-disease association. (HuGE Navigator) |
| 17727731 |
Observational study of gene-disease association. (HuGE Navigator) |
| 18191638 |
The results showed that the expression of Kir 4.1 mRNA and protein, as well as the Kir 4.1 immunoreactivity score (IRS), increased markedly with increasing pathologic grade. |
| 12401729 |
molecular analysis on chromosome 1q as a candidate gene for Type 2 diabetes in Pima Indians |
| 17122384 |
Calcium-sensing receptor interacts directly with Kir4.1 and Kir4.2 and can decrease their currents. |
| 15120748 |
Arg271Cys missense variation in KCNJ10 (or a nearby variation) is related to general seizure susceptibility in humans. |
| 15725393 |
Our results support previous evidence that the common KCNJ10 Arg271Cys missense variation influences seizure susceptibility of common IGE syndromes. | →View more information from publications. |
Recent Publications on KCNJ10: |  |
Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.
OBJECTIVE: The etiopathogenesis of temporal lobe epilepsy (TLE) and its... | 30th October, 2009
| Department of Neurology, Division of Clinical Neuroscience, Rikshospitalet
| Epilepsy Res. 2009 Oct 26.
DOI Direct Link |
Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats.
Currently, approximately 20 genetic variants are known to cause Mendelian... | 12th August, 2009
| The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, USA.
| Trends Genet. 2009 Aug;25(8):361-7. Epub 2009 Aug 6.
DOI Direct Link |
The EAST syndrome and KCNJ10 mutations.
Currently, approximately 20 genetic variants are known to cause Mendelian... | 12th August, 2009
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| N Engl J Med. 2009 Aug 6;361(6):630; author reply 630-1.
DOI Direct Link |
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss.
Noise-induced hearing loss (NIHL) is one of the leading occupational... | 7th August, 2009
| Department of Audiology and Phoniatrics, Nofer Institute of Occupational
| Ann Hum Genet. 2009 Jul;73(Pt 4):411-21.
DOI Direct Link |
Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex.
To determine the phenotypic significance of copy number changes (CNCs) in... | 23rd July, 2009
| Department of Medical Genetics, University Medical Center Utrecht,
| Eur J Hum Genet. 2009 Jul 22.
DOI Direct Link |
→View more research publications. |
KCNJ10 results (if any) from reagent suppliers | 
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P6610 Anti-Potassium Channel Kir4.1 antibody produced in rabbit ...
Gene Information, human ... KCNJ10(3766). rat ... Kcnj10(29718). mouse ... Kcnj10(16513). storage temp. −20°C. Safety. WGK Germany, 2. Related Products
...
http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=P661...
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KIR4.1 (G-19) Antibody sc-23637
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Human, KCNJ10, 3766, 1q23.2, NM_002241 ...
http://www.scbt.com/datasheet-23637-kir4-1-g-19-antibody.htm...
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Anti-Potassium Channel Kir4.1 antibody produced in rabbit (P6610 ...
Anti-Potassium Channel Kir4.1 (BIRK1, Kcnj10) is developed in rabbit using a highly purified peptide. (C)KLEESLREQAEKEGSALSVR , corresponding to ...
http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Datashee...
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Abgent - Neurosciences Antibodies
AT2597aNEW, KCNIP2 monoclonal antibody (M01), ELISA,IHC-P,RNAi-Ab,WB-Re,WB-Tr, H . AT2598aNEW, KCNJ10 monoclonal antibody (M01), ELISA,S-ELISA,WB-Re, H ...
http://www.abgent.com/products/category/neurosciences...
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Complete Solutions for Ion Channels
KCNJ10, NM_020269, potassium inwardly-rectifying channel: subfamily J: member 10 , P6610. KCNJ15, NM_019664, potassium inwardly-rectifying channel: subfamily ...
http://www.sigmaaldrich.com/life-science/functional-genomics...
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KCNQ1 (C-20) Antibody sc-10646
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. BMC Medicine. 2: 30. ...
http://www.scbt.com/ko/product.php?datasheet=10646&page=2...
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Abcam antibodies and reagents product map
... KCNH8 antibodies (2) · KCNIP1 antibodies (1) · KCNIP4 antibodies (2) · KCNJ10 antibodies (2) · KCNJ13 antibodies (1) · KCNJ15 antibodies (2) ...
http://www.abcam.com/index.html?cl=248&pageconfig=productmap...
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